HCID 11271378, compound → HCID 66702456, compound
Reaction equation
[Br:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([C:9]2[CH:10]=[C:11]([C:27]([NH2:29])=[O:28])[N:12]3[C:17]([NH:18][CH:19]([CH2:23][CH2:24][CH3:25])[CH2:20][CH2:21][CH3:22])=[CH:16][C:15]([CH3:26])=[N:14][C:13]=23)=[C:4]([CH3:30])[CH:3]=1.[ClH:31].C(OCC)(=O)C>C(O)C>[ClH:31].[Br:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([C:9]2[CH:10]=[C:11]([C:27]([NH2:29])=[O:28])[N:12]3[C:17]([NH:18][CH:19]([CH2:23][CH2:24][CH3:25])[CH2:20][CH2:21][CH3:22])=[CH:16][C:15]([CH3:26])=[N:14][C:13]=23)=[C:4]([CH3:30])[CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of 8-(4-bromo-2,6-dimethyl-phenyl)-2-methyl-4-(1-propyl-butylamino)-pyrrolo[1,2-a]pyrimidine-6-carboxylic acid amide (5.8 g) in ethanol (30 mL) was added 4 M HCl/ethyl acetate (3.7 mL) in an ice-cooling bath. The resulting solution was concentrated under reduced pressure. The residue was crystallized from ethyl acetate to give the title compound.
Workup
- temperaturecooling bath
- concentrationThe resulting solution was concentrated under reduced pressure
- customThe residue was crystallized from ethyl acetate
Sources & evidence
- ORD record
- ord-77911e6abf584bbab5668ec284e64f4c
- Source dataset
- uspto-grants-2012_01
- Patent number
- US08106194B2
Reaction notes
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